Rational Design of Fluorogenic and Spontaneously Blinking Labels for Super-Resolution Imaging

  • ACS Cent Sci. 2019 Sep 25;5(9):1602-1613. doi: 10.1021/acscentsci.9b00676.
Qinsi Zheng  1 Anthony X Ayala  1 Inhee Chung  1 Aubrey V Weigel  1 Anand Ranjan  2 Natalie Falco  1 Jonathan B Grimm  1 Ariana N Tkachuk  1 Carl Wu  2 Jennifer Lippincott-Schwartz  1 Robert H Singer  1  3 Luke D Lavis  1
Affiliations
  • 1. Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, Virginia 20147, United States.
  • 2. Department of Biology and Department of Molecular Biology and Genetics, Johns Hopkins University, Baltimore, Maryland 21218, United States.
  • 3. Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, New York 10461, United States.
Abstract

Rhodamine dyes exist in equilibrium between a fluorescent zwitterion and a nonfluorescent lactone. Tuning this equilibrium toward the nonfluorescent lactone form can improve cell-permeability and allow creation of "fluorogenic" compounds-ligands that shift to the fluorescent zwitterion upon binding a biomolecular target. An archetype fluorogenic dye is the far-red tetramethyl-Si-rhodamine (SiR), which has been used to create exceptionally useful labels for advanced microscopy. Here, we develop a quantitative framework for the development of new fluorogenic dyes, determining that the lactone-zwitterion equilibrium constant (K L-Z) is sufficient to predict fluorogenicity. This rubric emerged from our analysis of known fluorophores and yielded new fluorescent and fluorogenic labels with improved performance in cellular imaging experiments. We then designed a novel fluorophore-Janelia Fluor 526 (JF526)-with SiR-like properties but shorter fluorescence excitation and emission wavelengths. JF526 is a versatile scaffold for fluorogenic probes including ligands for self-labeling tags, stains for endogenous structures, and spontaneously blinking labels for super-resolution immunofluorescence. JF526 constitutes a new label for advanced microscopy experiments, and our quantitative framework will enable the rational design of Other fluorogenic probes for bioimaging.

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